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Tetracarboxylated Azobenzene/Polymer Supramolecular Assemblies as High-Performance Multiresponsive Actuators
被引:34
|作者:
Qin, Chengqun
[1
]
Feng, Yiyu
[1
,3
,4
]
An, Haoran
[1
]
Han, Junkai
[1
]
Cao, Chen
[1
]
Feng, Wei
[1
,2
,3
,4
]
机构:
[1] Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
[3] Minist Educ, Key Lab Adv Ceram & Machining Technol, Tianjin 300072, Peoples R China
[4] Tianjin Key Lab Composite & Funct Mat, Tianjin 300072, Peoples R China
基金:
中国国家自然科学基金;
关键词:
multistimuli-responsive polymers;
azobenzene;
polyelectrolytes;
supramolecular chemistry;
actuator;
CIS-TRANS ISOMERIZATION;
HIGH-ENERGY;
HOST-GUEST;
POLYMER;
FILMS;
LIGHT;
NANOCOMPOSITES;
CHROMOPHORES;
CRYSTALS;
HYBRIDS;
D O I:
10.1021/acsami.6b15075
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Multistimuli-responsive polymers are materials of emerging interest but synthetically challenging. In this work, supramolecular assembly was employed as a facile and effective approach for constructing 3,3',5,5'-azobenzenetetracarboxylic acid (H(4)abtc)/poly(diallyldimethylammonium chloride) (PDAC) supramolecules. Structural transformations of H(4)abtc can be induced by light, mechanical force, and heat and influenced by free volume. Thus, the fabricated free-standing H(4)abtc/PDAC film underwent bending/unbending movements upon treatment with light, humidity, or temperature, as asymmetric structural transformations on either side of the film generated asymmetric contraction/stretching forces. Fast rates of shape recovery were achieved for the film on exposure to gently flowing humid nitrogen. The bending/unbending motions are controllable, reversible, and repeatable. Hence, this light-, humido-, and thermo-responsive film has great potential in device applications for advanced functions.
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页码:4066 / 4073
页数:8
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